Ginsenoside Rg1 |
Panax ginseng |
CSE-induced COPD mice; Human embryonic lung fibroblasts exposed to CSE |
Suppressed airway fibrosis |
20 mg/kg |
In vivo
|
Guan et al. (2017a)
|
40 μM |
In vitro
|
CSE-induced COPD mice and HBE cells model |
Attenuated Pulmonary Epithelial-Mesenchymal Transition (EMT) |
5–20 mg/kg |
In vivo
|
Guan et al. (2017b)
|
5–160 μM |
In vitro
|
Ginsenoside Rg3 |
Panax ginseng |
AECOPD murine model established by CS exposure and NTHi infection; CS- and NTHi stimulation on BEAS-2B |
Inhibition of PI3K |
10–40 mg/kg |
In vivo
|
Guan et al. (2020)
|
10–160 μM |
In vitro
|
Salidroside |
Rhodiola rosea L |
CS-induced COPD in mice |
Mitigated skeletal muscle atrophy |
50–200 mg/kg |
In vivo
|
Zhang et al. (2019)
|
CS-induced COPD in mice |
Inhibition the MAPK/NF-kB pathway |
20–40 mg/kg |
In vivo
|
Luo et al. (2017)
|
Piscroside C |
Pseudolysimachion rotundum var. subintegrum |
TNF-α-stimulated human airway epithelial cells (NCI-H292 cells) |
Inhibited TNF-α/NF-κB pathway by suppression of PKCδ activity for TNF-RSC formation |
2.5–20 μM |
In vitro
|
Lee et al. (2018b)
|
CS- and LPS-induced COPD mice model; TNF-stimulated human airway epithelial NCIH292 cells |
Suppression of IKK/NF-κB activation |
15–30 mg/kg |
In vivo
|
Song et al. (2015)
|
2.5–20 μM |
In vitro
|
Naringin |
Grape fruit and citrus fruits |
CS-induced COPD mice model |
Anti-inflammatory |
20–80 mg/kg |
In vivo
|
Nie et al. (2012)
|
Paeoniflorin |
Paeonia lactiflora |
CS-exposed COPD mice model |
Attenuated oxidative stress via an Nrf2-dependent mechanism |
40 mg/kg |
In vivo
|
Lin et al. (2016)
|
Forsythiaside |
Forsythia suspensa |
CS-induced mice model |
Activating Nrf2 and inhibiting NF-κB signaling pathways |
15–60 mg/kg |
In vivo
|
Cheng et al. (2015)
|
Platycodin D |
Platycodon grandiflflorum |
CS-induced mice model |
Activating the Nrf2 signaling pathway |
20–80 mg/kg |
In vivo
|
Gao et al. (2017)
|
Saikosaponin a |
Radix bupleuri |
CS-induced mice model |
Inhibited oxidant stress and inflammatory by activating the Nrf2 and inhibiting the NF-κB signaling pathway |
5–20 mg/kg |
In vivo
|
Chen et al. (2018)
|